I 다이렉트자동차보험료비교견적사이트 ksuda Presents Encouraging IKS014 Phase 1 Data at …
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다이렉트자동차보험료비교견적사이트
다이렉트자동차보험료비교견적사이트 target="_blank" rel="nofollow noreferrer noopener">다이렉트자동차보험료비교견적사이트
다이렉트자동차보험료비교견적사이트
NEWCASTLE, ENGLAND--(Business Wire / Korea Newswire)--Iksuda Therapeutics (Iksuda), the developer of class leading, antibody drug conjugates (ADCs), today announces the presentation of new data from its Phase 1 study of IKS014, a human epidermal growth factor receptor 2 (HER2)-directed ADC, in patients with advanced HER2+ solid tumours.
The data was presented at the European Society for Medical Oncology (ESMO) Congress in Berlin, Germany.
The Phase 1 study (NCT05872295) is a non-randomised, open-label, multicentre trial evaluating IKS014 in patients with locally advanced or metastatic solid tumours that express HER2.
Part I, the dose escalation portion, is being conducted in sites in Australia and is designed to establish the maximum tolerated dose (MTD) and/or the recommended Phase 2 dose (RP2D) for IKS014 and provide initial safety, tolerability, efficacy, pharmacokinetic, pharmacodynamic and immunogenicity characteristics.
Part II dose expansion studies will assess IKS014 in HER2+ breast cancer in patients who have previously received Enhertu, HER2-low breast cancer, HER2+-gastric/ GEJ cancers and other HER2+ tumours and mutated HER2-NSCLC.
Dose expansion studies will be conducted in sites in the US, Australia, New Zealand and Singapore.
At the data cut-off date (31 July 2025), a total of 62 patients were enrolled in the study, with 55 patients evaluable for efficacy as measured by Response Evaluation Criteria in Solid Tumours (RECIST 1.1).
Anti-tumour activity was observed across all dose levels, with partial responses and unconfirmed partial responses observed in various tumour indications including breast, lung, oesophageal, ovarian, gastric, gallbladder and gastroesophageal junction cancers and in both HER2+ and HER2-low tumours.
Amongst 11 participants with breast cancer treated at doses >90mg/m2, seven responses were seen (objective response rate (ORR) 64%), including partial responses in all four patients with HER2+ disease.
Three of these patients had previously received Enhertu.
Additionally, amongst 10 patients with pre-treated, HER2+ oesophageal cancer that were enrolled across all dose levels, five achieved a response, including complete regression in one patient with non-measurable disease.
Treatment with IKS014 was generally well-tolerated at doses up to 120mg/m2 (~3.2 mg/kg), with anticipated adverse events including ocular surface AEs, pneumonitis and hypokalaemia, all of which were predominately Grade 1 and Grade 2.
An MTD was not reached per the study protocol.
Dose selection for further evaluation in the expansion cohorts will be based on preliminary activity, safety, pharmacokinetic, pharmacodynamic profile and overall benefit-risk assessment from the dose escalation.
The Phase 1 trial is expected to complete in H2 2026.
This data follows positive data from Phase 1 clinical trials through Fosun Pharma, which is now progressing FS-1502 (IKS014) through Phase 3 trials in China.[1] Dr.
Dave Simpson, Chief Executive Officer, Iksuda Therapeutics, commented: “We are hugely encouraged by these data, which illustrates the potential of IKS014 to improve outcomes and address the clinical unmet need across various HER-2 positive cancers, including treatment of those patients which are refractory to prior therapy options.” About IKS014 IKS014 is a potential best-in-class antibody drug conjugate, benefiting from tumour selective activation and release of the cytotoxic agent monomethyl auristatin F (MMAF).
In preclinical trials, it displayed impressive activity in high- and low-HER2 expressing tumours with a favourable Therapeutic Index compared with other HER2-directed drugs.
Iksuda gained exclusive world-wide rights (excluding Greater China and South Korea) to IKS014 from LigaChem Biosciences (https://iksuda.com/2022/01/iksuda-deepens-clinical-pipeline/).
About Iksuda Therapeutics: www.iksuda.com Iksuda Therapeutics is a clinical stage, UK-based biotechnology company focussed on the development of class leading antibody drug conjugates (ADCs) targeting difficult-to-treat haematological and solid tumours.
Iksuda’s pipeline of ADCs is centred on a portfolio of prodrug DNA and protein alkylating payloads in combination with stable conjugation chemistries including its proprietary PermaLink® platform.
The Company’s design concepts for ADCs are now clinically validated to significantly improve the therapeutic index of this important modality and improve the outcomes for patients living with cancer. 다이렉트자동차보험료비교견적사이트
[1] Li, Q., Cheng, Y., Tong, Z.
et al.
HER2-targeting antibody drug conjugate FS-1502 in HER2-expressing metastatic breast cancer: a phase 1a/1b trial.
Nat Commun 15, 5158 (2024).
https://doi.org/10.1038/s41467-024-48798-w View source version on businesswire.com: https://www.businesswire.com/news/home/20251019459034/en/ Website: https://iksuda.com/ Contact Iksuda Therapeutics Dave Simpson Chief Executive Officer +44 (0) 191 6031680 info@iksuda.com FTI Consulting (Financial Media and IR) Simon Conway / Rob Winder / Amy Byrne +44 (0) 020 3727 1000 Iksuda@fticonsulting.com This news is a press release provided by Iksuda Therapeutics.
Iksuda Therapeutics News Releases Iksuda Therapeutics announces first patient dosed in Phase 1 trial of IKS014 in patients with advanced solid tumours that express HER2 Iksuda Therapeutics (Iksuda), the developer of class leading antibody drug conjugates (ADCs) with enhanced tumour specificity, today announces that the first patient has completed a first cycle of therapy with IKS014, a human epidermal growth factor receptor 2 (HER2) ADC targeting patie...
2023년 10월 24일 16:25 익수다 테라퓨틱스, HER2 발현 진행성 고형종양 환자 대상 IKS014 임상 1상 시험에서 첫 환자 투약 발표 종양 특이성이 강화된 동급 선도적 항체 약물 결합체(ADC) 개발업체인 익수다 테라퓨틱스(Iksuda Therapeutics)가 진행성 HER2 양성 고형 종양 환자를 대상으로 한 인간 표피 성장 인자 수용체 2(HER2) ADC인 IKS014의 첫 환자가 첫 번째 치료 주기를 완료했다고 오늘 발표했다.
이는 현재 중국에서 임상 2상 ...
2023년 10월 24일 16:25 More News Health Clinical Trials Pharmaceutical R&D Overseas Iksuda Therapeutics Follow News Releases RSS Feed Website
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